类风湿关节炎新型靶向免疫生物学药物的系统综述:疗效、安全性和创新性

Sepideh Parchami Ghazaee, Kateryna Marchenko-Tolsta, Petro Sereda, M. Hameed, Sandra Lane
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引用次数: 0

摘要

在过去的半个世纪里,自身免疫性风湿病的治疗和管理得到了逐步改善,特别是随着被称为疾病修饰抗风湿药的免疫生物学或生物疗法的出现。尽管这些药物在治疗类风湿性关节炎(RA)方面普遍有效,但有些患者的疗效有限且对治疗无反应,此外,这些药物还可能引起不良临床反应,进一步加重病情。本综述旨在讨论新型治疗方法,为类风湿关节炎的未来指南和药物发现提供指导。本综述遵循2020年PRISMA声明,利用PubMed和谷歌学术进行文献检索,并强调近期关于靶向免疫生物学药物安全性和有效性的荟萃分析。小分子抑制剂,无论是单独使用还是与甲氨蝶呤联合使用,都已被证明有助于有效的疾病管理,并有可能更好地遵守美国风湿病学会的标准。与甲氨蝶呤联合使用时,托昔单抗疗法可显著减少疾病活动,提高疾病缓解率。间充质基质细胞疗法的研究取得了令人鼓舞的成果,既改善了软骨质量(通过宏观软骨修复评估),也改善了临床关节计数中的关节压痛和肿胀。耐受性树突状细胞的关节内给药能够减轻疼痛(通过视觉模拟量表评分),并提高 28 个关节的疾病活动度评分。更多的研究及其分析将改善患者的治疗效果,减少不良反应,降低开发和获取免疫生物药物的成本。此外,评估生物活性化合物抗 RA 特性的安全性和有效性,可以提供毒性更小、成本效益更高的天然治疗方案。
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A Systematic Review of the Novel Targeted Immunobiological Medications in Rheumatoid Arthritis: Efficacy, Safety, and Innovation
Over the last half-century, the treatment and management of autoimmune rheumatic diseases have progressively improved, particularly with the contribution of immunobiological or biological therapies known as disease-modifying antirheumatic drugs. Although these agents have been generally efficient in the management of rheumatoid arthritis (RA), some patients experience limited efficacy and non-responsiveness to treatment. In addition, they may cause adverse clinical effects, further aggravating the disease. Despite advancements in biological therapies, significant clinical needs persist. This review aims to discuss novel treatments, guiding future guidelines and drug discoveries for rheumatoid arthritis. This review follows the 2020 PRISMA statement, utilising PubMed and Google Scholar for literature search and emphasizing recent meta-analyses on the safety and efficacy of targeted immunobiological medications. Small molecule inhibitors, whether utilised independently or in conjunction with Methotrexate, have been shown to contribute to effective disease management and have the potential for better adherence to the American College of Rheumatology criteria. Tocilizumab therapy demonstrates a significant reduction in disease activity and improves rates of disease remission when combined with Methotrexate. Investigations of mesenchymal stromal cell therapies have had promising outcomes, improving both cartilage quality (as evaluated by Macroscopic Cartilage Repair Assessment) and joint tenderness and swelling in clinical joint counts. Intra-articular administration of tolerogenic dendritic cells has displayed a capacity to alleviate pain, as measured by Visual Analog Scale scores, and enhance the Disease Activity Score across 28 joints. Resveratrol capsules supplemented with allopathic therapy show potential in reducing TNF-α and interleukin-6 serum levels. More investigations and their analysis will improve patient outcomes and reduce adverse effects and the costs involved in developing and obtaining immunobiological drugs. Moreover, assessing the safety and efficacy of anti-RA properties of the bioactive compounds could offer less toxic and more cost-effective natural treatment options.
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